| Evolutionary and molecular facts link the WWC protein family to Hippo signaling DO Wennmann, J Schmitz, MC Wehr, MP Krahn, N Koschmal, ... Molecular biology and evolution 31 (7), 1710-1723, 2014 | 72 | 2014 |
| A deep learning approach to identify gene targets of a therapeutic for human splicing disorders D Gao, E Morini, M Salani, AJ Krauson, A Chekuri, N Sharma, ... Nature communications 12 (1), 3332, 2021 | 32 | 2021 |
| Topoisomerase IIβ associates with Ku70 and PARP-1 during double strand break repair of DNA in neurons R Mandraju, A Chekuri, C Bhaskar, K Duning, J Kremerskothen, ... Archives of biochemistry and biophysics 516 (2), 128-137, 2011 | 28 | 2011 |
| Glucotoxicity promotes aberrant activation and mislocalization of Ras-related C3 botulinum toxin substrate 1 [Rac1] and metabolic dysfunction in pancreatic islet β-cells … S Baidwan, A Chekuri, DAL Hynds, A Kowluru Apoptosis 22, 1380-1393, 2017 | 27 | 2017 |
| Late‐onset retinal degeneration pathology due to mutations in CTRP5 is mediated through HTRA1 A Chekuri, K Zientara‐Rytter, A Soto‐Hermida, S Borooah, ... Aging Cell 18 (6), e13011, 2019 | 26 | 2019 |
| IFT88 mutations identified in individuals with non-syndromic recessive retinal degeneration result in abnormal ciliogenesis A Chekuri, AA Guru, P Biswas, K Branham, S Borooah, A Soto-Hermida, ... Human genetics 137, 447-458, 2018 | 22 | 2018 |
| Long-Term Effects of Gene Therapy in a Novel Mouse Model of Human MFRP-Associated Retinopathy A Chekuri, B Sahu, VRM Chavali, M Voronchikhina, A Soto-Hermida, ... Human gene therapy 30 (5), 632-650, 2019 | 12 | 2019 |
| Analysis of gene expression during aging of CGNs in culture: implication of SLIT2 and NPY in senescence KP Gupta, PS Dholaniya, A Chekuri, AK Kondapi Age 37, 1-14, 2015 | 8 | 2015 |
| Selective retinal ganglion cell loss and optic neuropathy in a humanized mouse model of familial dysautonomia A Chekuri, EM Logan, AJ Krauson, M Salani, S Ackerman, EG Kirchner, ... Human Molecular Genetics 31 (11), 1776-1787, 2022 | 6 | 2022 |
| A deep learning approach to identify new gene targets of a novel therapeutic for human splicing disorders D Gao, E Morini, M Salani, AJ Krauson, A Ragavendran, S Erdin, ... BioRxiv, 2020.02. 03.932103, 2020 | 6 | 2020 |
| Development of an oral treatment that rescues gait ataxia and retinal degeneration in a phenotypic mouse model of familial dysautonomia E Morini, A Chekuri, EM Logan, JM Bolduc, EG Kirchner, M Salani, ... The American Journal of Human Genetics 110 (3), 531-547, 2023 | 5 | 2023 |
| Developmental regulation of neuronal gene expression by Elongator complex protein 1 dosage E Morini, D Gao, EM Logan, M Salani, AJ Krauson, A Chekuri, YT Chen, ... Journal of Genetics and Genomics 49 (7), 654-665, 2022 | 5 | 2022 |
| TopoisomeraseIIβ in HIV-1 transactivation A Chekuri, C Bhaskar, VS Bollimpelli, AK Kondapi Archives of Biochemistry and Biophysics 593, 90-97, 2016 | 5 | 2016 |
| Author Correction: Transcriptome analysis in a humanized mouse model of familial dysautonomia reveals tissue-specific gene expression disruption in the peripheral nervous system R Harripaul, E Morini, M Salani, E Logan, E Kirchner, J Bolduc, A Chekuri, ... Scientific reports 14 (1), 10103, 2024 | | 2024 |
| Transcriptome analysis in a humanized mouse model of familial dysautonomia reveals tissue-specific gene expression disruption in the peripheral nervous system R Harripaul, E Morini, M Salani, E Logan, E Kirchner, J Bolduc, A Chekuri, ... Scientific Reports 14 (1), 570, 2024 | | 2024 |
| Transcriptome analysis in a humanized mouse model of familial dysautonomia reveals tissue-specific gene expression disruption in the peripheral nervous system. D GAO, RS Harripaul, ES Morini, S Slaugenhaupt, A Chekuri, E Logan, ... | | 2023 |
| A Novel Mouse Model for Late-Onset Retinal Degeneration (L-ORD) Develops RPE Abnormalities Due to the Loss of C1qtnf5/Ctrp5 S Borooah, A Chekuri, S Pachauri, B Sahu, M Vorochikhina, JJ Suk, ... Retinal Degenerative Diseases XIX: Mechanisms and Experimental Therapy, 335-340, 2023 | | 2023 |
| Novel oral drug treatment rescues progressive optic neuropathy in a phenotypic mouse model of familial dysautonomia AK Chekuri, E Morini, E Logan, J Bolduc, E Kirchner, M Salani, A Krauson, ... Investigative Ophthalmology & Visual Science 64 (8), 3767-3767, 2023 | | 2023 |
| A blood-brain-barrier penetrant AAV gene therapy rescues neurological deficits in mucolipidosis IV mice. M Sangster, M Bishop, Y Yao, JF Feitor, S Shahriar, M Miller, A Chekuri, ... bioRxiv, 2023.11. 03.565568, 2023 | | 2023 |
| Development of a novel oral treatment that rescues gait ataxia and retinal degeneration in a phenotypic mouse model of familial dysautonomia E Morini, A Chekuri, EM Logan, JM Bolduc, EG Kirchner, M Salani, ... bioRxiv, 2022.11. 04.515198, 2022 | | 2022 |
MandrajuUT Southwestern Medical Center, Dallas.TexasVerified email at utsouthwestern.edu
